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Journal Abstract Search

162 related items for PubMed ID: 517576

  • 21. Prenatal diagnosis of congenital lipoid adrenal hyperplasia.
    Izumi H, Saito N, Ichiki S, Makino Y, Yukitake K, Kaneoka T.
    Obstet Gynecol; 1993 May; 81(5 ( Pt 2)):839-41. PubMed ID: 8469492
    [Abstract] [Full Text] [Related]

  • 22. Pitfalls in prenatal diagnosis of 21-hydroxylase deficiency by amniotic fluid steroid analysis? A six years experience in 102 pregnancies at risk.
    Forest MG.
    Ann N Y Acad Sci; 1985 May; 458():130-47. PubMed ID: 3879118
    [No Abstract] [Full Text] [Related]

  • 23. Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing.
    Pollack MS, Maurer D, Levine LS, New MI, Pang S, Duchon M, Owens RP, Merkatz IR, Nitowsky BM, Sachs G, Dupont B.
    Lancet; 1979 May 26; 1(8126):1107-8. PubMed ID: 86832
    [Abstract] [Full Text] [Related]

  • 24. Amniotic fluid steroid levels and fetal adrenal weight in congenital adrenal hyperplasia.
    Hughes IA, Dyas J, Laurence KM.
    Horm Res; 1987 May 26; 28(1):20-4. PubMed ID: 3502335
    [Abstract] [Full Text] [Related]

  • 25. Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Milunsky A, Tulchinsky D.
    Pediatrics; 1977 May 26; 59(5):768-70. PubMed ID: 558577
    [No Abstract] [Full Text] [Related]

  • 26. First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.
    Mornet E, Boue J, Raux-Demay M, Couillin P, Oury JF, Dumez Y, Dausset J, Cohen D, Boué A.
    Hum Genet; 1986 Aug 26; 73(4):358-64. PubMed ID: 3017844
    [Abstract] [Full Text] [Related]

  • 27. Amniotic fluid levels of 17 alpha-hydroxyprogesterone during human pregnancy: pre-natal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Wurster KG, Ranke MB, Heilbronner H, Gupta D.
    Endokrinologie; 1982 Oct 26; 80(2):142-50. PubMed ID: 6984387
    [Abstract] [Full Text] [Related]

  • 28. Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Morel Y, Miller WL.
    Adv Hum Genet; 1991 Oct 26; 20():1-68. PubMed ID: 1801590
    [No Abstract] [Full Text] [Related]

  • 29. Congenital adrenal hyperplasia.
    New MI, Levine LS.
    Monogr Endocrinol; 1984 Oct 26; 26():1-88. PubMed ID: 6472279
    [Abstract] [Full Text] [Related]

  • 30. [Progress in the prenatal diagnosis of adrenogenital syndrome].
    Blaim A.
    Ginekol Pol; 1984 Feb 26; 55(2):137-41. PubMed ID: 6381241
    [No Abstract] [Full Text] [Related]

  • 31. 11 Beta-hydroxylase deficiency congenital adrenal hyperplasia: update of prenatal diagnosis.
    Rösler A, Weshler N, Leiberman E, Hochberg Z, Weidenfeld J, Sack J, Chemke J.
    J Clin Endocrinol Metab; 1988 Apr 26; 66(4):830-8. PubMed ID: 3346360
    [Abstract] [Full Text] [Related]

  • 32. Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group.
    Levine LS, Zachmann M, New MI, Prader A, Pollack MS, O'Neill GJ, Yang SY, Oberfield SE, Dupont B.
    N Engl J Med; 1978 Oct 26; 299(17):911-5. PubMed ID: 692595
    [Abstract] [Full Text] [Related]

  • 33. Unusual heterozygotes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency confirmed by HLA tissue typing.
    Zachmann M, Prader A.
    Acta Endocrinol (Copenh); 1979 Nov 26; 92(3):542-6. PubMed ID: 517053
    [Abstract] [Full Text] [Related]

  • 34. HLA typing of amniotic cells: the prenatal diagnosis of congenital adrenal hyperplasia (21-OH-deficiency type).
    Pollack MS, Maurer D, Levine LS, New MI, Pang S, Duchon MA, Owens RP, Merkatz IR, Nitowsky HM, Sachs G, Dupont B.
    Transplant Proc; 1979 Dec 26; 11(4):1726-8. PubMed ID: 394430
    [No Abstract] [Full Text] [Related]

  • 35. [Congenital adrenal hyperplasia: 3 clinical forms in one family].
    Youlton R.
    Rev Med Chil; 1985 Dec 26; 113(12):1217-21. PubMed ID: 2942997
    [No Abstract] [Full Text] [Related]

  • 36. [Familial congenital adrenal hyperplasia caused by 11 beta-hydroxylase. Failure of prevention of sexual ambiguity and prenatal diagnosis].
    Bouchard M, Forest MG, David M, Dechaud H, Juif JG.
    Pediatrie; 1989 Dec 26; 44(8):637-40. PubMed ID: 2622705
    [Abstract] [Full Text] [Related]

  • 37. [Linkage between congenital adrenal hyperplasia with 21-hydroxylase deficiency and HLA histocompatibility groups].
    Cruz-Marin F, Raffoux C, Gilgenkrantz S, Janot C, Streiff F, Pierson M.
    J Genet Hum; 1981 Mar 26; 29(1):103-13. PubMed ID: 6977617
    [No Abstract] [Full Text] [Related]

  • 38. Congenital adrenal hyperplasia.
    Loke KY.
    J Singapore Paediatr Soc; 1991 Mar 26; 33(3-4):117-25. PubMed ID: 1812327
    [Abstract] [Full Text] [Related]

  • 39. [The eugenic significance of HLA determination in congenital adrenal hyperplasia].
    Li XQ.
    Zhonghua Yi Xue Za Zhi; 1984 Feb 26; 64(2):105-7. PubMed ID: 6432246
    [No Abstract] [Full Text] [Related]

  • 40. Prenatal diagnosis of a heterozygote of salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency by genetic linkage analysis.
    Oh BH, Park JK, Choi YM, Yang IM, Kim YS, Choi YK.
    J Korean Med Sci; 1988 Jun 26; 3(2):73-7. PubMed ID: 3267357
    [Abstract] [Full Text] [Related]

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